meddevicedb.com FDA Device Reference

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER WITH BALLOON

K911630 Class II Traditional
Decision Date
1991-09-27
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K911630
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 1991-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER WITH BALLOON received FDA 510(k) clearance under submission number K911630, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1991-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.